In this paper we report centered 6 x 2 [c(6 x 2)] and centered 4 x 2 [c(4 x
2)] reconstructions of SrTiO3(001) surfaces observed consistently using lo
w energy electron diffraction and high resolution scanning tunneling micros
copy. We find that the final ordering of the SrTiO3(001) surface depends no
t only on the annealing conditions, but also critically on the surface cond
ition before ultra-high vacuum annealing. Auger electron spectroscopy measu
rements revealed a systematic correlation of AES intensity ratio I(Sr)/I(Ti
) and I(O)/I(Ti) with various types of reconstructed surface [1 x 1, 2 x 1,
c(4 x 2), and c(6 x 2)]. It also shows roughly a linear dependence of O-to
-Ti ratio on the Sr-to-Ti ratio. Therefore, the change in stoichiometry dri
ves the surface to different superstructures. We discuss the surface electr
onic states associated with the oxygen vacancies, and their effect on the e
lectron tunneling. The c(6 x 2) surface is found to be extremely stable in
ultra-high vacuum, even during atomic resolution scanning tunneling microsc
opic imaging. A single domain c(6 x 2) reconstruction can be stabilized on
a vicinal (001) surface. (C) 1999 Elsevier Science B.V. All rights reserved
.